Alunbrig (brigatinib) vs Gavreto (pralsetinib)

Alunbrig (brigatinib) vs Gavreto (pralsetinib)

Alunbrig (brigatinib) and Gavreto (pralsetinib) are both targeted therapies used to treat non-small cell lung cancer (NSCLC) with specific genetic mutations. Alunbrig is designed to inhibit anaplastic lymphoma kinase (ALK) and is used in patients who have ALK-positive metastatic NSCLC, particularly after crizotinib resistance or intolerance. Gavreto targets rearranged during transfection (RET) proto-oncogene alterations and is indicated for the treatment of NSCLC with RET fusion-positive tumors, as well as for certain types of thyroid cancer with RET mutations or fusions. Patients should consult with their healthcare provider to determine the most appropriate medication based on the specific genetic alterations of their cancer, the drug's efficacy, potential side effects, and overall treatment plan.

Difference between Alunbrig and Gavreto

Metric Alunbrig (brigatinib) Gavreto (pralsetinib)
Generic name Brigatinib Pralsetinib
Indications ALK-positive metastatic non-small cell lung cancer (NSCLC) RET fusion-positive non-small cell lung cancer (NSCLC), RET-mutant medullary thyroid cancer (MTC), and RET fusion-positive thyroid cancer
Mechanism of action Anaplastic lymphoma kinase (ALK) inhibitor RET kinase inhibitor
Brand names Alunbrig Gavreto
Administrative route Oral Oral
Side effects Nausea, diarrhea, fatigue, cough, headache Constipation, hypertension, fatigue, musculoskeletal pain, diarrhea
Contraindications Hypersensitivity to brigatinib Hypersensitivity to pralsetinib
Drug class Tyrosine kinase inhibitor Tyrosine kinase inhibitor
Manufacturer Takeda Pharmaceuticals U.S.A., Inc. Blueprint Medicines Corporation

Efficacy

Efficacy of Alunbrig (brigatinib) in Lung Cancer

Alunbrig (brigatinib) is a medication that has been approved for the treatment of non-small cell lung cancer (NSCLC) with specific genetic alterations, namely anaplastic lymphoma kinase (ALK) positive mutations. The efficacy of Alunbrig in treating this type of lung cancer was demonstrated in several clinical trials. One pivotal trial that led to its approval was the ALTA-1L study, which showed that brigatinib significantly improved progression-free survival compared to crizotinib, another ALK inhibitor, in patients with ALK-positive NSCLC who had not received prior treatment. Patients treated with brigatinib experienced a median progression-free survival of around 24 months, compared to approximately 11 months for those on crizotinib.

Additionally, brigatinib has shown high intracranial efficacy in patients with brain metastases, a common complication of ALK-positive NSCLC. In clinical trials, a substantial proportion of patients with measurable brain metastases at baseline achieved complete or partial responses, suggesting that Alunbrig is effective in controlling central nervous system disease, which is a significant concern in this patient population.

Efficacy of Gavreto (pralsetinib) in Lung Cancer

Gavreto (pralsetinib) is another targeted therapy approved for the treatment of NSCLC, specifically for patients with rearranged during transfection (RET) fusion-positive tumors. The approval of Gavreto was based on results from the ARROW clinical trial, which demonstrated that pralsetinib had significant antitumor activity in patients with RET fusion-positive NSCLC. The trial reported an overall response rate of approximately 70% in treatment-naive patients and around 60% in those who had undergone prior therapy, indicating that Gavreto is highly effective in inducing tumor responses in this patient population.

In addition to its efficacy in shrinking tumors, Gavreto has also shown a durable response, with many patients experiencing prolonged periods of disease control. This is particularly important for patients with RET fusion-positive NSCLC, as this genetic alteration is associated with a poor prognosis and limited treatment options. The introduction of Gavreto provides a new targeted therapy option that can lead to significant improvements in outcomes for these patients.

Regulatory Agency Approvals

Alunbrig
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Gavreto
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

Access Alunbrig or Gavreto today

If Alunbrig or Gavreto are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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